Luxar Corp.
FDA 510(k) & PMA Approved Devices — 17 products
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Total Devices17
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K960475 | MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM | GEX | 1996-04-26 | View |
| 510(k) | K953074 | MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM | GEX | 1995-08-28 | View |
| 510(k) | K945888 | MODIFIED LUXAR LX-20 FAMILY C02 LASER SYSTEM | GEX | 1995-01-27 | View |
| 510(k) | K904068 | LUXAR MODEL LX-20 CO2 LASER | GEX | 1991-04-15 | View |
| 510(k) | K903079 | ENDOGUIDE (R), MICROGUIDE (TM), FLEXIGUIDE (TM) | GEX | 1990-10-04 | View |
| 510(k) | K900066 | FLEXIGUIDE(TM) CO2 LASER HOLLOW FLEXIBLE FIBER | GEX | 1990-03-19 | View |
| 510(k) | K897040 | LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (NEURO.) | GEX | 1990-02-13 | View |
| 510(k) | K896478 | LUXAR MODEL LX-20 MINILASE CO2 LASER | GEX | 1990-02-08 | View |
| 510(k) | K896618 | LIST GENERAL SURGERY AS INTENDED USE FOR ENDOGUIDE | GEX | 1990-01-09 | View |
| 510(k) | K896619 | LIST DERMATOLOGY/PLASTIC SURGERY AS USE ENDOGUIDE | GEX | 1990-01-09 | View |
| 510(k) | K896711 | LISTING PODIATRY AS INTENDED USE FOR ENDOGUIDE | GEX | 1990-01-09 | View |
| 510(k) | K896595 | LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE | GEX | 1990-01-09 | View |
| 510(k) | K896617 | LISTING ENT AS INTENDED USE FOR ENDOGUIDE | GEX | 1990-01-09 | View |
| 510(k) | K895786 | ENDOGUIDE PRODUCT LINE: EX0120, EX0300 AND EX0400 | GEX | 1989-10-27 | View |
| 510(k) | K895559 | MODIFIED ENDOGUIDE | GEX | 1989-10-20 | View |
| 510(k) | K893642 | MODIFIED ENDOGUIDE | GEX | 1989-07-14 | View |
| 510(k) | K884459 | LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE | GEX | 1988-12-19 | View |
No matching devices.
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